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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368642Generated: November 1, 2026

Sodium borohydride → HCID 58119742, compound

https://huagongshe.com/reaction/2368642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58119718HCID 58119718—
SolventEthanolHCID 702—
ProductHCID 58119742HCID 58119742—

Reaction Conditions

Temperature70 °C

Reaction Steps

959 mg (6) Benzyl 4-((5S)-5-(tert-butyldimethylsilyloxy)-2-(1-methoxyethyl)-7,7-dimethyl-3-(4-(trifluoromethyl)benzoyl)-5,6,7,8-tetrahydroquinolin-4-yl)piperidine-1-carboxylate (Example VI (69) are dissolved in 15 ml ethanol. To the mixture 441 mg of sodiumborohydride is added. The reaction is stirred for 2 hours at 70° C. Then 8 equivalents of sodiumborohydride are added and the reaction is stirred over night at 70° C. The solvent is evaporated under vacuum. Water, ethylacetate and 1M hydrochloric acid are added. The aqueous phase is extracted with ethylacetate and the combined organic phases are washed with brine. After drying with natrium sulphate the solvents are evaporated under vacuum and the residue is chromatographed on isolate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703793B2
Source datasetuspto-grants-2014_04
ORD IDord-0cbdeebce609487db45703cbde4c6979
Source noteuspto-grants-2014_04